Abstract

Herein, g-C3N4/CdS hybrids with controllable CdS nanoparticles anchoring on g-C3N4 nanosheets were constructed. The effects of CdS nanoparticles on photocatalytic H2 production and organic molecule degradation for g-C3N4/CdS hybrids were investigated. The maximum rate of H2 production for g-C3N4/CdS sample was 1,070.9 μmol g−1 h−1, which was about four times higher than that of the individual g-C3N4 nanosheet sample. The enhanced photocatalytic performance for prepared hybrids could be mainly attributed to the following causes: the formed heterojunctions can contribute to the light absorption and separation of photogenerated electrons and holes, the two-dimensional layered structure facilitates the transmission and transfer of electrons, and high specific surface area could provide more exposed active sites.

Highlights

  • Semiconductor materials have received widespread attention as promising photocatalysts for clean energy production and environmental problems. (Tong et al, 2012; Chang et al, 2016; Yu et al, 2017; Qi et al, 2018; Cao et al, 2019; Ng et al, 2021)

  • In order to optimize the photocatalytic performances of g-C3N4/CdS hybrids, some important factors should be taken into account, such as effective contact between two components, well-controlled morphology structure and particle size, and sufficiently exposed reactive active sites

  • The synthesis processes of g-C3N4/CdS hybrids are shown in Scheme 1

Read more

Summary

Introduction

Semiconductor materials have received widespread attention as promising photocatalysts for clean energy production and environmental problems. (Tong et al, 2012; Chang et al, 2016; Yu et al, 2017; Qi et al, 2018; Cao et al, 2019; Ng et al, 2021). In order to optimize the photocatalytic performances of g-C3N4/CdS hybrids, some important factors should be taken into account, such as effective contact between two components, well-controlled morphology structure and particle size, and sufficiently exposed reactive active sites.

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call